Phase I clinical and pharmacological study of suppression of human antimouse antibody response to monoclonal antibody L6 by deoxyspergualin

Cancer Res. 1995 Jul 15;55(14):3060-7.

Abstract

Development of human antimouse antibody (HAMA) is a major limiting factor in the application of murine mAb for clinical use. A novel immunomodulatory drug, deoxyspergualin (DSG), has shown potential to suppress antimouse antibody response in preclinical model systems. We conducted a Phase I trial to determine the effect of DSG on HAMA response to murine mAb L6 administered to patients with advanced cancers (in previous trials, this antibody elicited HAMA in two-thirds of the treated patients). L6 mAb was administered at a fixed dose of 200 mg/m2 on days 1-5. DSG was administered at doses of 50 mg/m2 [dose level (dl) 1] or 150 mg/m2 (dls II and III) on days 1-7. Treatment courses were repeated every 6 weeks (dls I and II) or every 3 weeks (dl III). HAMAs were quantitated by a commercially available ELISA assay (ImmuSTRIP; anti-isotypic antibodies) and a radiometric assay (antiisotypic and anti-idiotypic antibodies). Pharmacokinetics of L6 and DSG was also studied in all consenting patients. Among 24 evaluable patients, 2 patients developed detectable HAMAs using the ELISA (one each at dls I and II) after a median follow-up of 122 days (P = 0.0001 as compared to historical controls). Even in the two patients who developed HAMA, the HAMA levels were quite low (160 and 181 ng/ml; historical experience, 70-38,744 ng/ml). The radiometric assay detected anti-L6 antibodies in 13 patients (4, 6, and 3 at dls I-III, respectively) after a median of 82 days. The median highest anti-L6 antibody level was 129 ng/ml (range, 21-2150). The highest anti-L6 antibody level at dl III was only 44 ng/ml. The results suggest suppression of anti-idiotypic response also. No clinical antitumor activity was observed, and no significant changes in T4/T8 subsets or immunoglobulins occurred (suggesting a lack of generalized immunosuppression). We conclude that DSG can suppress HAMA response to L6. A starting dose of 150 mg/m2/day is recommended for Phase II trials to confirm this observation.

Publication types

  • Clinical Trial
  • Clinical Trial, Phase I
  • Comparative Study
  • Controlled Clinical Trial
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Aged
  • Antibiotics, Antineoplastic / adverse effects
  • Antibiotics, Antineoplastic / pharmacokinetics
  • Antibiotics, Antineoplastic / pharmacology*
  • Antibodies, Anti-Idiotypic / biosynthesis*
  • Antibodies, Monoclonal / adverse effects
  • Antibodies, Monoclonal / drug effects*
  • Antibodies, Monoclonal / pharmacology*
  • Antibody Formation / drug effects
  • Complement Activation / drug effects
  • Complement C3 / metabolism
  • Complement C4 / metabolism
  • Dose-Response Relationship, Drug
  • Drug Interactions
  • Female
  • Guanidines / adverse effects
  • Guanidines / pharmacokinetics
  • Guanidines / pharmacology*
  • Humans
  • Isoantigens / immunology
  • Isoantigens / pharmacology
  • Male
  • Middle Aged
  • Neoplasms / drug therapy*
  • Neoplasms / immunology*

Substances

  • Antibiotics, Antineoplastic
  • Antibodies, Anti-Idiotypic
  • Antibodies, Monoclonal
  • Complement C3
  • Complement C4
  • Guanidines
  • Isoantigens
  • gusperimus